A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526496



Internal ID15453789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11390648..11397837hg38UCSC Ensembl
Innerchr10:11432647..11439836hg19UCSC Ensembl
Innerchr10:11472653..11479842hg18UCSC Ensembl
Innerchr10:11472653..11479842hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387190
hg197190
hg187190
hg177190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702805
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526496
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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